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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947117copy number variation1nstd209human GRCh38 chr12: 57,061,436-57,061,742 , GRCh37.p13 chr12: 57,455,219-57,455,525 NEMP1
    nsv5938198copy number variation1nstd209human GRCh38 chr12: 57,076,382-57,076,659 , GRCh37.p13 chr12: 57,470,165-57,470,442 NEMP1
    nsv5511155copy number variation1nstd206human GRCh38 chr12: 57,077,166-57,080,381 , GRCh37.p13 chr12: 57,470,949-57,474,164 NEMP1
    nsv5503663copy number variation1nstd206human GRCh38 chr12: 57,081,975-57,082,848 , GRCh37.p13 chr12: 57,475,758-57,476,631 NEMP1
    nsv5278155copy number variation1nstd204human GRCh38.p13 chr12: 57,065,501-57,078,300 , GRCh37.p13 chr12: 57,459,284-57,472,083 NEMP1
    nsv5215077mobile element deletion1nstd204human GRCh38.p13 chr12: 57,074,283-57,074,597 , GRCh37.p13 chr12: 57,468,066-57,468,380 NEMP1
    nsv5139613mobile element insertion1nstd203human GRCh38 chr12: 57,066,836-57,066,852 , GRCh37.p13 chr12: 57,460,619-57,460,635 NEMP1
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4972911copy number variation1nstd200human GRCh38 chr12: 57,075,727-57,077,807 , GRCh37.p13 chr12: 57,469,510-57,471,590 NEMP1
    nsv4899793mobile element deletion1nstd200human GRCh38 chr12: 57,074,293-57,074,588 , GRCh37.p13 chr12: 57,468,076-57,468,371 NEMP1
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4775098mobile element deletion1nstd200human GRCh37 chr12: 57,468,076-57,468,371 , GRCh38.p12 chr12: 57,074,293-57,074,588 NEMP1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4705451copy number variation1nstd195human GRCh37 chr12: 57,458,855-57,458,856 , GRCh38.p12 chr12: 57,065,072-57,065,073 NEMP1
    nsv4675143copy number variation1nstd102humanPathogenic GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523 OR6C71P, METTL1, 183 more genes
    nsv4527675copy number variation1nstd166human GRCh37.p13 chr12: 57,460,186-57,460,591 , GRCh38.p12 chr12: 57,066,403-57,066,808 NEMP1
    nsv4512241mobile element insertion1nstd166human GRCh37.p13 chr12: 57,460,619-57,460,619 , GRCh38.p12 chr12: 57,066,836-57,066,836 NEMP1
    nsv4501371mobile element insertion1nstd166human GRCh37.p13 chr12: 57,460,131-57,460,131 , GRCh38.p12 chr12: 57,066,348-57,066,348 NEMP1
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